Clinical Trial Manager | Expression of interest - Australia or New Zealand

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Clinical Trial Manager - Make an Impact at the Forefront of Innovation The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer. The Clinical Trial Manager interprets data on project issues and makes good business decisions with the goal of ensuring timely and cost-effective delivery of high-quality clinical trial results. This role is responsible for managing multiple clinical trials simultaneously, ensuring compliance with regulatory requirements, maintaining accurate records, and providing regular updates to stakeholders. Key responsibilities include: • Developing and implementing effective study management plans, including timelines, budgets, and resource allocation. • Coordinating and collaborating with cross-functional teams, including clinical research associates, data coordinators, and other stakeholders. • Ensuring compliance with regulatory requirements, including Good Clinical Practice (GCP), International Conference on Harmonisation (ICH) guidelines, and local regulations. • Managing and maintaining accurate records of study progress, including patient enrollment, data collection, and outcome measures. • Providing regular updates to stakeholders, including sponsors, investigators, and other team members. • Identifying and resolving project issues in a timely manner, with minimal impact on the overall project timeline. The Clinical Trial Manager will work closely with the Study Manager and other study team members to ensure successful delivery of clinical trials. This role requires strong organizational skills, attention to detail, and excellent communication and interpersonal skills. The ideal candidate will have: • A degree in a life science or related field (e.g., biology, chemistry, pharmacology). • At least 3 years of experience in clinical trial management, preferably with a focus on pharmaceutical or biotechnology companies. • Strong understanding of regulatory requirements, including GCP and ICH guidelines. • Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams. • Ability to prioritize tasks and manage multiple projects simultaneously. • Strong attention to detail and organizational skills, with the ability to maintain accurate records and track progress. • Familiarity with electronic data capture (EDC) systems and other clinical trial management tools.